Aurobindo Pharma Limited - Urgent Openings in Production / Engineering / Analytical QA - Apply Now

Urgent Openings in Production / Engineering / Analytical QA

Technical Assistant – Production (Pharma Formulations – OSD)

Location: Hyderabad

Job Description:

Operation of Compression, capsule filling, coating and Granulation

·         Review of E-BMR

·         cGMP compliance for the Production area

·         Preparation, review, training of standard operating procedures

·         Production activities-Planning daily, weekly and monthly.

·         To ensure the conformance of systems and work practices with the SOP.

Required Candidate profile

Production with min 2-8yrs experience in Pharma Mfg - Formulations

Preferably in (Tablet, capsules) with

1.     Qualification: ITI/Diploma/Any Graduate

2.     Granulation,Capsule filling,Compression

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Executive – Engineering (Documentation) Pharma Formulations

Job Description:

Engineering Document compliance (QMS)

Preparing of CCF, CAPA, QRM and investigation for deviations

Preparation and revision of engineering SOP

Review of engineering schedules -PM, calibration filter cleaning...

Required Candidate profile

Engineering (Maintenance) with min 2-6 yrs experience in Pharma formulations pref. in Sterile Injectables having experience in

Documentation

QMS (Engineering document compliance)

Preparation of CCF, CAPA, QRM

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Analytical QA – Executive (Pharma Formulations OSD)

Experience: 3-8 yrs

Job Description:
Review of analytical reports Raw material, Packing material, In process, Stability study, analytical method validation protocols/ reports, Calibration, instrument qualification, Working standard qualification, analyst qualification etc. for compliance of the data as per statutory

Verifications of Certificate of analysis

Responsible for Review of QMS Documents (e.g. OOS, OOT, Incident, Deviation and Change control).

Responsible for review of electronic data to ensure the data Attributable, Legible, Contemporaneous, Original & Accurate.

Responsible to handle regulatory inspections

Review of SOP's related to Quality Control.

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